Prenatal exposure to lamotrigine: effects on postnatal development and behaviour in rat offspring. 2014

Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
Centre for Toxicology and Developmental Research (CEFT), Sri Ramachandra University, Chennai, Tamil Nadu 600116, India.

Use of antiepileptic drugs (AEDs) in pregnancy warrants various side effects and also deleterious effects on fetal development. The present study was carried out to assess the effects of prenatal exposure to lamotrigine (LTG) on postnatal development and behavioural alterations of offspring. Adult male and female Sprague Dawley rats weighing 150-180 g b. wt. were allowed to copulate and pregnancy was confirmed by vaginal cytology. Pregnant rats were treated with LTG (11.5, 23, and 46 mg/kg, p.o) from gestational day 3 (GND 3) and this treatment continued till postnatal day 11 (PND 11). Offspring were separated from their dam on day 21 following parturition. LTG, at 46 mg/kg, p.o, produced severe clinical signs of toxicity leading to death of dam between GND 15 and 17. LTG, at 11.5 and 23 mg/kg, p.o, showed significant alterations in offspring's incisors eruption and vaginal opening when compared to age matched controls. LTG (23 mg/kg, p.o) exposed female offspring expressed hyperactive behaviour and decreased GABA-A receptor expression when compared to control rats. These results reveal that prenatal exposure to LTG may impart differential postnatal behavioural alterations between male and female rats which paves way for further investigations.

UI MeSH Term Description Entries

Related Publications

Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
December 2015, International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience,
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
April 2012, Birth defects research. Part B, Developmental and reproductive toxicology,
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
November 1999, Behavioural pharmacology,
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
January 2021, Environmental toxicology and pharmacology,
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
November 2009, Reproductive toxicology (Elmsford, N.Y.),
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
January 2004, Neurotoxicology and teratology,
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
December 1988, Pharmacological research communications,
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
January 2005, Neurotoxicology and teratology,
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
January 2007, Growth, development, and aging : GDA,
Sekar Sathiya, and Murugan Ganesh, and Periyathambi Kalaivani, and Vijayan Ranju, and Srinivasan Janani, and Bakthavachalam Pramila, and Chidambaram Saravana Babu
February 2023, Toxicology letters,
Copied contents to your clipboard!